VACUETTE EVACUATED BLOOD COLLECTION TUBES

VACUETTE EVACUATED BLOOD COLLECTION TUBES is an FDA 510(k)-cleared medical device (K011699) manufactured by Greiner Bio-One Vacuette North America. This device is classified under the Clinical Chemistry specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 27, 2001. Regulation: 8.